A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv528n21



Internal ID22766720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121396133..121518605hg38UCSC Ensembl
chrX:120529987..120652459hg19UCSC Ensembl
chrX:120357668..120480140hg18UCSC Ensembl
chrX:120255522..120377994hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38122473
hg19122473
hg18122473
hg17122473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520087, nsv523353
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv528n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer